Published November 24, 2020
| Version v1
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TGFBI case WES variants
Description
Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report
Data of VCF of three affected members who shared a phenotype of corneal dystrophy in different stages of severity
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- Is supplement to
- Journal article: 10.21203/rs.3.rs-24728/v5 (DOI)